Validation Engineer: GMP/QA Pharmaceutical Systems
Listed on 2026-09-25
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Quality Assurance - QA/QC
Quality Engineering -
Pharmaceutical
Pharma Engineer, Quality Engineering
Commissioning Partners seeks a motivated Validation Engineer to support validation and qualification activities in a GMP-regulated pharmaceutical environment. You will develop and execute validation documents for equipment, facilities, utilities, and computerized systems.
Responsibilities include preparing URS, FDS, IQ/OQ/PQ protocols, writing test scripts, executing qualification testing, and ensuring ALCOA+ data integrity. Collaboration with Engineering, Manufacturing, QA, and IT is essential.
As a Validation Engineer: GMP/QA for Pharmaceutical Systems, you will play an important part at Commissioning Partners in KY, United States.
Join Commissioning Partners and contribute to our ongoing work.
Take a moment to read everything above and see whether this role is right for you.
This posting is for the Validation Engineer: GMP/QA for Pharmaceutical Systems role at Commissioning Partners, based in KY, United States.
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